| Literature DB >> 11801640 |
Diana Zelenika1, Elizabeth Adams, Sue Humm, Luis Graca, Sara Thompson, Stephen P Cobbold, Herman Waldmann.
Abstract
There is now compelling evidence for subpopulations of CD4+ T cells whose role is to prevent immune pathology in both autoimmunity and transplantation. We have cloned CD4+ T cells against a male transplantation Ag that, unlike Th1 or Th2 clones, suppresses the rejection of male skin grafts and are therefore considered examples of regulatory T cells. We have identified, using serial analysis of gene expression, transcripts that are overexpressed in regulatory T cells compared with Th1 and Th2 clones. Some of these transcripts are increased in tolerated rather than rejecting skin grafts and in addition are expressed by the natural regulatory CD4+CD25+ subpopulation of naive mice. These genes include prepro-enkephalin, GM2 ganglioside activator protein, glucocorticoid-induced TNFR superfamily member 18, and integrin alpha(E)beta(7). They seem to represent a subset of transcripts shared with Th2 cells, suggesting that transplantation tolerance and normal immunoregulation may represent a unique form of Th2-like differentiation.Entities:
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Year: 2002 PMID: 11801640 DOI: 10.4049/jimmunol.168.3.1069
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422